Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_provenance.
- NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_assertion description "[The autosomal dominantly inherited condition familial hypocalciuric hypercalcemia (FHH) is characterized by elevated plasma calcium levels, relative or absolute hypocalciuria, and normal to moderately elevated plasma PTH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_provenance.
- NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_assertion evidence source_evidence_literature NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_provenance.
- NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_assertion SIO_000772 17698911 NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_provenance.
- NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_assertion wasDerivedFrom befree-2016 NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_provenance.
- NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_assertion wasGeneratedBy ECO_0000203 NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_provenance.
- befree-2016 importedOn "2016-02-19" NP625094.RAxED408llqia-uMqg9isfsLXWy86JJlVxF-Mgr65EJgw130_provenance.